Trityl chloride → HCID 54453593, compound
Reaction equation
[C:1]1([C:7]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)Cl)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH:21][N:22]1[C:26](=[O:27])[C:25]([CH:31]=[CH:32][CH3:33])([CH:28]=[CH:29][CH3:30])[C:24]([CH:37]=[CH:38][CH3:39])([CH:34]=[CH:35][CH3:36])[C:23]1=[O:40].C(N(CC)CC)C>CN(C)C=O>[C:7]([O:21][N:22]1[C:26](=[O:27])[C:25]([CH:31]=[CH:32][CH3:33])([CH:28]=[CH:29][CH3:30])[C:24]([CH:34]=[CH:35][CH3:36])([CH:37]=[CH:38][CH3:39])[C:23]1=[O:40])([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
0.14 mole of triphenylchloromethane and 0.14 mole of N-hydroxy tetrapropenylsuccinimide are dissolved in 100 milliliters of dimethylformamide. 50 milliliters of triethylamine are added and the mixture is stirred overnight at room temperature. The solvent is then removed under vacuum and the reaction product is water washed until salt free and then dried. A yield of 90% of N-trityloxy tetrapropenylsuccinimide is recovered.
Workup
- customThe solvent is then removed under vacuum
- washwashed until salt free
- customdried
Sources & evidence
- ORD record
- ord-b4b846194e054343a1ca0b38a0b49389
- Source dataset
- uspto-grants-1978_08
- Patent number
- US04104182
Reaction notes
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